Nom du produit:5-bromo-2-methylthiophene-3-carboxylic acid

IUPAC Name:5-bromo-2-methylthiophene-3-carboxylic acid

CAS:1344027-40-2
Formule moléculaire:C6H5BrO2S
Pureté:95%
Numéro de catalogue:CM199508
Poids moléculaire:221.07

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CM199508-250mg in stock ȌȷƋ
CM199508-1g in stock ɐDzɐ

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Détails du produit

N° CAS:1344027-40-2
Formule moléculaire:C6H5BrO2S
Point de fusion:-
Code SMILES:O=C(C1=C(C)SC(Br)=C1)O
Densité:
Numéro de catalogue:CM199508
Poids moléculaire:221.07
Point d'ébullition:
N° Mdl:MFCD20278363
Stockage:Keep in dark place, store in freezer, under -20°C.

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

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Product Other Information

Product Overview 5-Bromo-2-methylthiophene-3-carboxylic acid (5-BrMTCA) is a sulfur-containing carboxylic acid that has been studied extensively for its potential applications in scientific research. 5-BrMTCA is a versatile compound that is used in the synthesis of various compounds.
Synthesis and Application 5-Bromo-2-methylthiophene-3-carboxylic acid is synthesized through a reaction between 5-bromo-2-methylthiophene and acetic anhydride. This reaction produces 5-bromo-2-methylthiophene-3-carboxylic acid, which is then isolated by crystallization. The synthesis of 5-Bromo-2-methylthiophene-3-carboxylic acid is a simple and cost-effective process. 5-Bromo-2-methylthiophene-3-carboxylic acid is widely used in scientific research for its versatile properties.
Future Directions Future research on 5-Bromo-2-methylthiophene-3-carboxylic acid should focus on further elucidating the mechanism of action and pharmacodynamics of the compound. Additionally, future research should focus on exploring the potential therapeutic applications of 5-Bromo-2-methylthiophene-3-carboxylic acid, such as its ability to inhibit the formation of lipid peroxidation products and its anti-inflammatory properties. Additionally, future research should focus on exploring the potential of 5-Bromo-2-methylthiophene-3-carboxylic acid in the treatment of various diseases, such as cancer and cardiovascular diseases. Finally, future research should focus on exploring the potential of 5-Bromo-2-methylthiophene-3-carboxylic acid in the development of new drugs and drug delivery systems.